Quinns Advantage Thaw Kit

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name: Quinns Advantage Thaw Kit FDA UDI
Generic Name: IVF medium kit FDA UDI
Device Name: Quinns Advantage Thaw Kit. 3x12 ml FDA UDI
Model / Reference: ART-8016 FDA UDI
Description: Quinns Advantage Thaw Kit. 3x12 ml FDA UDI

Identifiers

Primary DI / UDI-DI: 60888937819306 FDA UDI
FDA Product Code: MQL FDA UDI
GMDN Term: IVF medium kit FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.6180 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: IVF medium kit

Quinns Advantage Thaw Kit by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as IVF medium kit.

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G-Vitri™ Warming media — Gimbo Medical Technology Shenzhen Co., Ltd. · Class II
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Vitrification Media(VS solution) — KITAZATO CORPORATION · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: CooperSurgical, Inc.

Sources (1)

FDA UDI d898d449-4587-4aac-bd71-8d8610164555 34 fields · synced Jun 9, 2026